Canonical Allele Identifier: CA2625844049
Gene: POMT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77286861A>G , CM000676.2:g.77286861A>G GRCh38
NC_000014.8:g.77753204A>G , CM000676.1:g.77753204A>G GRCh37
NC_000014.7:g.76822957A>G NCBI36
NG_008897.1:g.39022T>C , LRG_844:g.39022T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000556394.2:c.795-39T>C ENSP00000451967.2:n.795-39T>C
ENST00000682247.1:c.1254-39T>C ENSP00000507213.1:n.1254-39T>C
ENST00000682382.1:c.826-39T>C
ENST00000682395.1:n.1393T>C
ENST00000682459.1:n.957-39T>C
ENST00000682467.1:c.1254-39T>C ENSP00000508062.1:n.1254-39T>C
ENST00000682706.1:n.31-39T>C
ENST00000682795.1:c.1254-39T>C ENSP00000507574.1:n.1254-39T>C
ENST00000682895.1:n.970-39T>C
ENST00000682955.1:n.542-39T>C
ENST00000683188.1:c.1190T>C
ENST00000683328.1:c.247-39T>C ENSP00000508096.1:n.247-39T>C
ENST00000683380.1:n.918-39T>C
ENST00000683828.1:c.963-39T>C
ENST00000684259.1:n.1105-39T>C
ENST00000684549.1:n.805-39T>C
ENST00000261534.9:c.1254-39T>C MANE Select ENSP00000261534.4:n.1254-39T>C
ENST00000261534.8:c.1254-39T>C ENSP00000261534.4:n.1254-39T>C
ENST00000452340.7:n.1277-39T>C
ENST00000553880.5:n.125-39T>C
ENST00000554767.5:n.2040-39T>C
ENST00000554884.5:n.246-39T>C
ENST00000556404.1:n.349T>C
ENST00000556851.1:n.290-39T>C
ENST00000557675.5:n.344-39T>C
NM_013382.5:c.1254-39T>C , LRG_844t1:c.1254-39T>C NP_037514.2:n.1254-39T>C
XM_011536675.1:c.1254-39T>C XP_011534977.1:n.1254-39T>C
XM_011536676.1:c.921-39T>C XP_011534978.1:n.921-39T>C
XM_011536677.1:c.795-39T>C XP_011534979.1:n.795-39T>C
XM_011536678.1:c.1254-39T>C XP_011534980.1:n.1254-39T>C
XM_011536679.1:c.348-39T>C XP_011534981.1:n.348-39T>C
XM_011536680.1:c.*368T>C XP_011534982.1:n.*368T>C
XR_943416.1:n.1457-39T>C
XM_011536675.2:c.1254-39T>C XP_011534977.1:n.1254-39T>C
XM_011536676.2:c.921-39T>C XP_011534978.1:n.921-39T>C
XM_011536677.3:c.795-39T>C XP_011534979.1:n.795-39T>C
XR_001750279.1:n.1454-39T>C
XR_001750282.1:n.1868T>C
XR_943416.3:n.1455-39T>C
NM_013382.6:c.1254-39T>C NP_037514.2:n.1254-39T>C
NM_013382.7:c.1254-39T>C MANE Select NP_037514.2:n.1254-39T>C